Canonical Allele Identifier: PA111495
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13267
ClinVar RCV Id: RCV000014181 RCV000014182 RCV000014183 RCV000415484 RCV000655416 RCV000490034
ClinVar Variation Id: 374820
ClinVar RCV Id: RCV000415499 RCV000560038 RCV000856727 RCV001729573 RCV003155177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Cys342Ser
CA256746
NM_000141.5:c.1024T>A
CA10575447
NM_000141.5:c.1025G>C
CA2695212875
NM_000141.5:c.1025_1026delinsCT